The following data is part of a premarket notification filed by Pb Diagnostic Systems, Inc. with the FDA for Opus (tm) Hcg.
| Device ID | K901935 |
| 510k Number | K901935 |
| Device Name: | OPUS (TM) HCG |
| Classification | Visual, Pregnancy Hcg, Prescription Use |
| Applicant | PB DIAGNOSTIC SYSTEMS, INC. 151 UNIVERSITY AVE. Westwood, MA 02090 |
| Contact | Lori Baranauskas |
| Correspondent | Lori Baranauskas PB DIAGNOSTIC SYSTEMS, INC. 151 UNIVERSITY AVE. Westwood, MA 02090 |
| Product Code | JHI |
| CFR Regulation Number | 862.1155 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-04-30 |
| Decision Date | 1990-06-26 |